| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:19380162-19380349 | Common:5; Rare:96 | ||||
| chr9:20684099-20684288 | Common:3; Rare:76 | ||||
| chr9:21031571-21031665 | Common:1; Rare:45 | ||||
| chr9:21335338-21335504 | Common:3; Rare:60 | ||||
| chr9:26892418-26892534 | Rare:61 | ||||
| chr9:26892713-26892891 | Common:1; Rare:86 | ||||
| chr9:26947140-26947256 | Rare:40 | ||||
| chr9:26956249-26956497 | Common:2; Rare:93 | ||||
| chr9:27573426-27573530 | Common:5; Rare:55 | ||||
| chr9:32552553-32552688 | Common:1; Rare:26; Clinvar:2 | ||||
| chr9:32573048-32573271 | Common:4; Rare:85 | ||||
| chr9:33001585-33001746 | Common:3; Rare:76; Clinvar (benign):3 | ||||
| chr9:33025090-33025342 | Common:7; Rare:108 | ||||
| chr9:33076590-33076855 | Common:2; Rare:83 | ||||
| chr9:33264699-33265124 | Rare:117 |